Canonical Allele Identifier: CA2672740349

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.176687574C>A , CM000666.2:g.176687574C>A GRCh38
NC_000004.11:g.177608728C>A , CM000666.1:g.177608728C>A GRCh37
NC_000004.10:g.177845722C>A NCBI36
NG_034216.1:g.110172G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000618562.2:c.812-54G>T (VEGFC) MANE Select ENSP00000480043.1:n.812-54G>T
ENST00000618562.1:c.812-54G>T (VEGFC) ENSP00000480043.1:n.812-54G>T
NM_005429.4:c.812-54G>T (VEGFC) NP_005420.1:n.812-54G>T
XR_939498.1:n.260+7824C>A (HAFML)
XR_939499.1:n.209+17865C>A (HAFML)
XR_939498.2:n.347+7824C>A (HAFML)
XR_939499.2:n.292+17865C>A (HAFML)
NM_005429.5:c.812-54G>T (VEGFC) MANE Select NP_005420.1:n.812-54G>T